Reacción #310320

ord-862eea4fe61a46a7a4bd37ce9962335e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was refluxed for 15 hours
  2. 2
    Filtraciónfiltered
  3. 3
    Concentraciónthe filtrate was concentrated in-vacuo
  4. 4
    Otroto give a viscous oil as residue
  5. 5
    OtroRecrystallization from isopropyl alcohol

Procedimiento

To a solution of 3.0 g (0.02 mole) 4-hydroxy-6-methyl-2-trichloromethylpyrimidine and 1.3 g (0.02 mole) triethylamine in 75 ml diethyl ether was added 1.4 g (0.02 mole) crotonyl chloride. The reaction mixture was refluxed for 15 hours and filtered, and the filtrate was concentrated in-vacuo to give a viscous oil as residue. Trituration with petroleum ether caused the oil to solidify. Recrystallization from isopropyl alcohol gave 1.8 g (45% yield) of pure product; m.p. 55° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04352806uspto-grants-1982_10